Blennow E - Search Results

1

Molecular and clinical characterization of patients with overlapping 10p deletions.

Lindstrand A, Malmgren H, Verri A, Benetti E, Eriksson M, Nordgren A, Anderlid BM, Golovleva I, Schoumans J, Blennow E. Lindstrand A, et al. Among authors: blennow e. Am J Med Genet A. 2010 May;152A(5):1233-43. doi: 10.1002/ajmg.a.33366. Am J Med Genet A. 2010. PMID: 20425828

2

Subtelomeric rearrangements detected in patients with idiopathic mental retardation.

Anderlid BM, Schoumans J, Annerén G, Sahlén S, Kyllerman M, Vujic M, Hagberg B, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: blennow e. Am J Med Genet. 2002 Feb 1;107(4):275-84. doi: 10.1002/ajmg.10029. Am J Med Genet. 2002. PMID: 11840483

3

FISH-mapping of a 100-kb terminal 22q13 deletion.

Anderlid BM, Schoumans J, Annerén G, Tapia-Paez I, Dumanski J, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: blennow e. Hum Genet. 2002 May;110(5):439-43. doi: 10.1007/s00439-002-0713-7. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073014

4

Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): deletion/duplication of 7q33-34 and clinical correlations.

Malmgren H, Malm G, Sahlén S, Karlsson M, Blennow E. Malmgren H, et al. Among authors: blennow e. Am J Med Genet A. 2005 Nov 15;139(1):25-31. doi: 10.1002/ajmg.a.30983. Am J Med Genet A. 2005. PMID: 16222668

5

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review.

Malmgren H, Sahlén S, Wide K, Lundvall M, Blennow E. Malmgren H, et al. Among authors: blennow e. Am J Med Genet A. 2007 Sep 15;143A(18):2143-9. doi: 10.1002/ajmg.a.31902. Am J Med Genet A. 2007. PMID: 17696125

6

Chimerism resulting from parthenogenetic activation and dispermic fertilization.

Winberg J, Gustavsson P, Lagerstedt-Robinson K, Blennow E, Lundin J, Iwarsson E, Nordenström A, Anderlid BM, Bondeson ML, Nordenskjöld A, Nordgren A. Winberg J, et al. Among authors: blennow e. Am J Med Genet A. 2010 Sep;152A(9):2277-86. doi: 10.1002/ajmg.a.33594. Am J Med Genet A. 2010. PMID: 20803645

7

Inherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: inter- and intra-individual variation and correlation to the phenotype.

Kvarnung M, Lindstrand A, Malmgren H, Thåström A, Jacobson L, Dahl N, Lundin J, Blennow E. Kvarnung M, et al. Among authors: blennow e. Am J Med Genet A. 2012 May;158A(5):1111-7. doi: 10.1002/ajmg.a.35311. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495764

8

Maternal isodisomy of chromosome 9 with no impact on the phenotype in a woman with two isochromosomes: i(9p) and i(9q).

Björck EJ, Anderlid BM, Blennow E. Björck EJ, et al. Among authors: blennow e. Am J Med Genet. 1999 Nov 5;87(1):49-52. doi: 10.1002/(sici)1096-8628(19991105)87:1<49::aid-ajmg10>3.0.co;2-4. Am J Med Genet. 1999. PMID: 10528247

9

Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy.

Anderlid BM, Sahlén S, Schoumans J, Holmberg E, Ahsgren I, Mortier G, Speleman F, Blennow E. Anderlid BM, et al. Among authors: blennow e. Am J Med Genet. 2001 Mar 15;99(3):223-33. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1146>3.0.co;2-w. Am J Med Genet. 2001. PMID: 11241494

10

Concurrent microdeletion and duplication of 22q11.2.

Blennow E, Lagerstedt K, Malmgren H, Sahlén S, Schoumans J, Anderlid B. Blennow E, et al. Clin Genet. 2008 Jul;74(1):61-7. doi: 10.1111/j.1399-0004.2008.01008.x. Epub 2008 Apr 28. Clin Genet. 2008. PMID: 18445048

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